Canonical Allele Identifier: CA4137440

Gene: AP5Z1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.4785008C>T , CM000669.2:g.4785008C>T	GRCh38
NC_000007.13:g.4824639C>T , CM000669.1:g.4824639C>T	GRCh37
NC_000007.12:g.4791165C>T	NCBI36
NG_028111.1:g.14378C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014855.3:c.891C>T MANE Select	NP_055670.1:p.Ala297=
ENST00000649063.2:c.891C>T MANE Select	ENSP00000497815.1:p.Ala297=
NM_001364858.1:c.423C>T	NP_001351787.1:p.Ala141=
NM_014855.2:c.891C>T	NP_055670.1:p.Ala297=
NR_157345.1:n.984C>T
ENST00000348624.4:c.891C>T	ENSP00000297562.4:p.Ala297=
ENST00000477680.5:n.649C>T
ENST00000477680.6:n.649C>T
ENST00000491375.1:n.746C>T
ENST00000496303.5:n.955C>T
ENST00000496303.6:n.719C>T
ENST00000647628.1:n.382C>T
ENST00000647984.1:c.*236C>T	ENSP00000497794.1:n.*236C>T
ENST00000648925.1:c.891C>T	ENSP00000496830.1:p.Ala297=
ENST00000649315.1:c.101C>T
ENST00000649419.1:n.98C>T
ENST00000650310.1:c.891C>T	ENSP00000497395.1:p.Ala297=
XR_242109.1:n.916C>T